Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
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HPO disease - gene - phenotype typical associations: |
HPO disease - gene - phenotype less frequent non-typical associations: |
HP:0003710 | HP:0003710 | Exercise-induced muscle cramps | 0 | ATP2A1 CL E G H | 487 | 811 | OMIM:601003 | BRODY MYOPATHY | | | | 80 | | |
HP:0003710 | HP:0003710 | Exercise-induced muscle cramps | 0 | CAV3 CL E G H | 859 | 1529 | OMIM:123320 | Creatine phosphokinase, elevated serum | . | | | 148 | | |
HP:0003710 | HP:0003710 | Exercise-induced muscle cramps | 0 | CAV3 CL E G H | 859 | 1529 | OMIM:606072 | Rippling muscle disease | . | | | 148 | | |
HP:0003710 | HP:0003710 | Exercise-induced muscle cramps | 0 | CHCHD10 CL E G H | 400916 | 15559 | ORPHA:276435 | Lower motor neuron syndrome with late-adult onset | HP:0040282 - Frequent | | | 11 | | |
HP:0003710 | HP:0003710 | Exercise-induced muscle cramps | 0 | CPT2 CL E G H | 1376 | 2330 | ORPHA:228302 | Carnitine palmitoyl transferase II deficiency, myopathic form | HP:0040283 - Occasional | | | 101 | | |
HP:0003710 | HP:0003710 | Exercise-induced muscle cramps | 0 | CPT2 CL E G H | 1376 | 2330 | ORPHA:228305 | Carnitine palmitoyl transferase II deficiency, severe infantile form | HP:0040282 - Frequent | | | 101 | | |
HP:0003710 | HP:0003710 | Exercise-induced muscle cramps | 0 | DMD CL E G H | 1756 | 2928 | ORPHA:206546 | Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers | | | | 1496 | | |
HP:0003710 | HP:0003710 | Exercise-induced muscle cramps | 0 | HINT1 CL E G H | 3094 | 4912 | ORPHA:324442 | Autosomal recessive axonal neuropathy with neuromyotonia | HP:0040282 - Frequent | | | 12 | | |
HP:0003710 | HP:0003710 | Exercise-induced muscle cramps | 0 | LAMA2 CL E G H | 3908 | 6482 | OMIM:618138 | MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23; LGMDR23 | | | | 411 | | |
HP:0003710 | HP:0003710 | Exercise-induced muscle cramps | 0 | LAMP2 CL E G H | 3920 | 6501 | OMIM:300257 | Danon disease | . | | | 211 | | |
HP:0003710 | HP:0003710 | Exercise-induced muscle cramps | 0 | MLIP CL E G H | 90523 | 21355 | OMIM:620138 | | | | | | | |
HP:0003710 | HP:0003710 | Exercise-induced muscle cramps | 0 | PFKM CL E G H | 5213 | 8877 | OMIM:232800 | Glycogen storage disease VII | . | | | 64 | | |
HP:0003710 | HP:0003710 | Exercise-induced muscle cramps | 0 | PGAM2 CL E G H | 5224 | 8889 | OMIM:261670 | Phosphoglycerate mutase, muscle, deficiency of | . | | | 26 | | |
HP:0003710 | HP:0003710 | Exercise-induced muscle cramps | 0 | PGK1 CL E G H | 5230 | 8896 | OMIM:300653 | Phosphoglycerate kinase 1 deficiency | . | | | 21 | | |
HP:0003710 | HP:0003710 | Exercise-induced muscle cramps | 0 | PYGL CL E G H | 5836 | 9725 | ORPHA:369 | Glycogen storage disease due to liver glycogen phosphorylase deficiency | HP:0040283 - Occasional | | | 71 | | |
HP:0003710 | HP:0003710 | Exercise-induced muscle cramps | 0 | PYGM CL E G H | 5837 | 9726 | ORPHA:368 | Glycogen storage disease due to muscle glycogen phosphorylase deficiency | HP:0040282 - Frequent | | | 166 | | |
HP:0003710 | HP:0003710 | Exercise-induced muscle cramps | 0 | PYGM CL E G H | 5837 | 9726 | OMIM:232600 | Glycogen storage disease V | | | | 166 | | |
HP:0003710 | HP:0003710 | Exercise-induced muscle cramps | 0 | RYR1 CL E G H | 6261 | 10483 | ORPHA:466650 | Exercise-induced malignant hyperthermia | HP:0040283 - Occasional | | | 1200 | | |
HP:0003710 | HP:0003710 | Exercise-induced muscle cramps | 0 | SLC16A1 CL E G H | 6566 | 10922 | OMIM:245340 | Erythrocyte lactate transporter defect | . | | | 74 | | |
HP:0003710 | HP:0008991 | Exercise-induced leg cramps | 1 | HINT1 CL E G H | 3094 | 4912 | ORPHA:324442 | Autosomal recessive axonal neuropathy with neuromyotonia | HP:0040283 - Occasional | | | 12 | | |